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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 877294생성일: 2026년 10월 25일

Diphenylamine → 4-(Diphenylamino)benz[a]anthracene

https://huagongshe.com/reaction/877294

반응식

참여 물질

역할이름HCID투입량
반응물DiphenylamineHCID 11487—
반응물Di-tert-butylchlorophosphineHCID 139566—
반응물Benz(a)anthracene, 4-bromo-HCID 182324—
반응물Sodium t-butoxideHCID 23676156—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물4-(Diphenylamino)benz[a]anthraceneHCID 59412792—

반응 조건

온도60 °C

반응 단계

190 μl (1 mmol) of chlorodi-tert-butylphosphine and then 112 mg (0.5 mmol) of palladium(II) acetate are added to a suspension of 15.4 g (50 mmol) of 4-bromobenz[a]anthracene, 10.2 g (60 mmol) of diphenylamine and 7.7 g (80 mmol) of sodium tert-butoxide in 500 ml of toluene, and the mixture is subsequently heated under reflux for 5 h. After the mixture has been cooled to 60° C., 500 ml of water are added, the organic phase is separated off, filtered through silica gel, evaporated virtually to dryness at 80° C. in vacuo, and 300 ml of ethanol are then added. After cooling, the solid is filtered off with suction. Recrystallisation five times from dioxane (about 8 ml/g); sublimation (p=5×10−5 mbar, T=280° C.). Yield: 12.7 g (32 mmol), 64.1%, purity 99.9% (HPLC), Tg=74.7° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08986852B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-3d424e238af145848f7273db027f9b8e
출처 메모uspto-grants-2015_03